- ¥1000
- HZbscienc
- 中国/欧洲/美国
- HZ0341
- 2025年07月08日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
-20摄氏度保存
- 保质期：
1年
- 英文名：
pSilencer 3.1-H1 neo
- 库存：
大量
- 供应商：
上海沪震生物科技有限公司
- 规格：
盒
pSilencer 3.1-H1 neo产品信息
订购信息
| 货号 | 载体名称 | 出品公司 | 载体用途 | 价格 | 到货周期 |
| HZ0341 | pSilencer 3.1-H1 neo | RNAi载体 | 1000 | 现货 |
载体描述
The pSilencer vectors employ RNA polymerase III (pol III) promoters which generate large amounts of small RNA using relatively simple promoter and terminator sequences. They also include an antibiotic resistance gene that provides a mechanism to select for transfected cells that express the introduced DNA.
载体序列
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文献和实验U6 vector, nucleotide overhangs to the EcoR I and Apa I restriction sites are added to the 5' and 3' end of the DNA oligonucleotides, respectively (Figure 2). In contrast, for cloning into the pSilencer 2.0-U6, 2.1-U6, 3.0-H1, or 3.1-H1 vectors
are added to the 5' and 3' end of the DNA oligonucleotides, respectively (Figure 2). In contrast, for cloning into the pSilencer 2.0-U6, 2.1-U6, 3.0-H1, or 3.1-H1 vectors, nucleotide overhangs with Bam H I and Hin d III restriction sites are added
(Figure 2). In contrast, for cloning into the pSilencer 2.0-U6, 2.1-U6, 3.0-H1, or 3.1-H1 vectors, nucleotide overhangs with BamH I and Hind III restriction sites are added to the 5' and 3' end of the DNA oligonucleotides, respectively (Figure
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